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(+/-)-cis-1-(4-Chlorphenyl)-2-methyl-ethylenoxid, also known as (±)-cis-1-(4-chlorophenyl)-2-methyl-1-propene oxide, is a chiral organic compound with the molecular formula C10H11ClO. It is a colorless liquid that is derived from the epoxidation of 1-(4-chlorophenyl)-2-methyl-1-propene, a compound containing a 4-chlorophenyl group and a methyl group. This chemical is characterized by its cis-configuration, which means that the chlorine atom and the methyl group are on the same side of the double bond. It is an important intermediate in the synthesis of various pharmaceuticals and agrochemicals due to its unique structural features. The compound is sensitive to heat and light, and it is typically stored under controlled conditions to maintain its stability.

1886-50-6

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1886-50-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1886-50-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,8,8 and 6 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1886-50:
(6*1)+(5*8)+(4*8)+(3*6)+(2*5)+(1*0)=106
106 % 10 = 6
So 1886-50-6 is a valid CAS Registry Number.

1886-50-6Downstream Products

1886-50-6Relevant academic research and scientific papers

OXADIAZINE COMPOUNDS AND METHODS OF USE THEREOF

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, (2017/03/14)

The present disclosure relates to oxadiazine compounds, pharmaceutical compositions comprising an effective amount of an oxadiazine compound and methods for using an oxadiazine compound in the treatment of a neurodegenerative disease, comprising administering to a subject in need thereof an effective amount of an oxadiazine compound.

Synthesis of enantiopure 2-amino-1-phenyl and 2-amino-2-phenyl ethanols using enantioselective enzymatic epoxidation and regio- and diastereoselective chemical aminolysis

Sello, Guido,Orsini, Fulvia,Bernasconi, Silvana,Gennaro, Patrizia Di

, p. 372 - 376 (2007/10/03)

Several enantiopure 1,2-amino alcohols have been prepared by combining a stereoselective enzymatic epoxidation of styrenes with regio- and stereoselective chemical reactions. An interesting reactivity has been noted concerning the reaction of epoxides and NH3 under microwave activation.

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